HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyridinecarboxaldehyde → 4-Benzyl-1-(pyridin-2-ylmethylidene)thiosemicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | 3-Amino-1-benzylthiourea | HCID 737135 | — |
| Product | 4-Benzyl-1-(pyridin-2-ylmethylidene)thiosemicarbazide | HCID 1550383 | — |
Reaction Steps
The title compound was prepared from a mixture of 4-benzylthiosemicarbazide (100 mg, 0.552 mmol) and 2-pyridinecarboxaldehyde (52 μL, 0.552 mmol) similar to Example 3 and isolated as a pale white solid (83 mg, 59%). 1H NMR (DMSO-d6): 11.84 (s, 1H), 9.27 (t, J=5.7 Hz, 1H), 8.57 (d, J=4.8 Hz, 1H), 8.30 (d, J=8.1 Hz, 1H), 8.13 (s, 1H), 7.83 (t, J=7.7 Hz, 1H), 7.40-7.31 (m, 3H), 7.26 (d, J=4.8 Hz, 1H), 4.86 (d, J=6.0 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794400B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-136ea58e3b8d43c0a0e061aab5423271 |
| Source note | uspto-grants-2004_09 |